<p>(A) 293FT cells (left) and M2-293FT cells (right) were cell surface stained with the human anti-M2 Ab1-10 mAb (upper panel) and the mouse anti-M2 14C2 mAb (lower panel) and analyzed by flow cytometry. Shaded histograms represent unstained cells. The binding of the isotype controls (dotted line) and anti-M2e specific mAbs (black line) is shown. (B) Uninfected A549 (left) and influenza infected (right) A549-H1N1 cells were cell surface stained with the human anti-M2 Ab1-10 mAb. The binding of secondary Ab alone (grey histogram) and the binding of Ab1-10 mAb (black line histogram) is shown.</p
<p><b>(A-B)</b> Binding of O157 3F10 and O145 4C8 mAbs to <i>E</i>.<i>coli</i> O157 <b>(A)</b> or <i...
<p><b>A</b>.MS17-57 bound to all four GC cell lines that were used for live cell immunization. <b>B<...
<p>Cell ELISA assay was performed on CHO cells expressing WT and mutant (Y465D) ACE using the panel ...
<p>CEM-4 cells were incubated for 2 h at 4°C with gp120<sub>MN</sub> (0.24 µg/ml) or with no gp120 (...
<p>A mouse anti-<i>B mallei</i> IgG1was used (10 µg/ml) as an isotype mAb control, and the mouse ant...
<p>The mouse anti-<i>B mallei</i> IgG1 (panel A) was used as a nonspecific isotype control. The mous...
Abstract Background Matrix protein 2 (M2) is an integral tetrameric membrane protein of influenza A ...
<p>Macrophages from wildtype (A) or <i>ABCA1<sup>−/−</sup></i> (B) mice were stained with anti-annex...
The highly conserved matrix protein 2 (M2) is a good candidate for the development of a broadly prot...
<p>(A) Effectors (freshly isolated NK cells) and targets (293FT and M2-293FT cells) were co-incubate...
<p>(A) Uninfected CEM-4 cells, (B) CEM-4 cells infected with HIV-1 clade B. Cells were incubated, as...
<div><p>The highly conserved matrix protein 2 (M2) is a good candidate for the development of a broa...
<p>The left panels (A, B, C) are monomeric and dimeric BsAbs (EphA10/CD3) and the central panels (D,...
<p>(A, B) mAbs created from PR8 pre-exposed mice that were boosted either with PR8 (A) or S12a (B) w...
<p>Monoclonal Abs 61D3 and MEM18 were tested for reactivity against wild-type CD14 and a panel of po...
<p><b>(A-B)</b> Binding of O157 3F10 and O145 4C8 mAbs to <i>E</i>.<i>coli</i> O157 <b>(A)</b> or <i...
<p><b>A</b>.MS17-57 bound to all four GC cell lines that were used for live cell immunization. <b>B<...
<p>Cell ELISA assay was performed on CHO cells expressing WT and mutant (Y465D) ACE using the panel ...
<p>CEM-4 cells were incubated for 2 h at 4°C with gp120<sub>MN</sub> (0.24 µg/ml) or with no gp120 (...
<p>A mouse anti-<i>B mallei</i> IgG1was used (10 µg/ml) as an isotype mAb control, and the mouse ant...
<p>The mouse anti-<i>B mallei</i> IgG1 (panel A) was used as a nonspecific isotype control. The mous...
Abstract Background Matrix protein 2 (M2) is an integral tetrameric membrane protein of influenza A ...
<p>Macrophages from wildtype (A) or <i>ABCA1<sup>−/−</sup></i> (B) mice were stained with anti-annex...
The highly conserved matrix protein 2 (M2) is a good candidate for the development of a broadly prot...
<p>(A) Effectors (freshly isolated NK cells) and targets (293FT and M2-293FT cells) were co-incubate...
<p>(A) Uninfected CEM-4 cells, (B) CEM-4 cells infected with HIV-1 clade B. Cells were incubated, as...
<div><p>The highly conserved matrix protein 2 (M2) is a good candidate for the development of a broa...
<p>The left panels (A, B, C) are monomeric and dimeric BsAbs (EphA10/CD3) and the central panels (D,...
<p>(A, B) mAbs created from PR8 pre-exposed mice that were boosted either with PR8 (A) or S12a (B) w...
<p>Monoclonal Abs 61D3 and MEM18 were tested for reactivity against wild-type CD14 and a panel of po...
<p><b>(A-B)</b> Binding of O157 3F10 and O145 4C8 mAbs to <i>E</i>.<i>coli</i> O157 <b>(A)</b> or <i...
<p><b>A</b>.MS17-57 bound to all four GC cell lines that were used for live cell immunization. <b>B<...
<p>Cell ELISA assay was performed on CHO cells expressing WT and mutant (Y465D) ACE using the panel ...